Hybrid metal oxide cycle water splitting

ABSTRACT

Hybrid thermochemical water splitting systems are disclosed that thermally reduces metal oxides particles to displace some but not all of the electrical requirements in a water splitting electrolytic cell. In these hybrid systems, the thermal reduction temperature is significantly reduced compared to two-step metal-oxide thermochemical cycles in which only thermal energy is required to produce hydrogen from water. Also, unlike conventional higher temperature systems where the reduction step must be carried out under reduced oxygen pressure, the reduction step in the proposed hybrid systems can be carried out in air, allowing for thermal input by a solar power tower with a windowless, cavity receiver.

CROSS REFERENCE TO RELATED APPLICATION

This application is a divisional of U.S. application Ser. No. 14/115,095, entitled “HYBRID METAL OXIDE CYCLE WATER SPLITTING,” filed on Oct. 31, 2013, which is a 35 U.S.C. 371 national stage application of PCT International Application No. PCT/US2011/001340 filed Jul. 29, 2011, which claims priority to U.S. Provisional Application Ser. No. 61/368,756, filed on Jul. 29, 2010, all of which are hereby incorporated by reference in their entireties.

BACKGROUND OF THE DISCLOSURE

The present disclosure relates generally to methods and apparatus associated with hybrid metal oxide cycle water splitting.

SUMMARY OF THE INVENTION

In one aspect of the disclosure, a hybrid thermochemical splitting cycle implementation is disclosed that includes a reactive particle receiver including an open cavity, a down comer, a hot particle storage container, a heat exchanger, and an electrolyzer. The oxidized particles are directly heated and thermally reduced in the open cavity. Within the hybrid thermochemical splitting cycle implementation, a hybrid thermochemical splitting cycle is performed that includes thermally reducing a metal oxide with concentrated solar energy and reoxidizing an oxygen-deficient metal oxide in an electrochemical cell, wherein the chemical potential for the reactions is provided by the metal oxide and electrical energy, and wherein the electrical energy required is significantly lower than needed for water or carbon dioxide electrolysis alone.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a schematic view of a hybrid metal oxide cycle; and

FIG. 2 shows one implementation strategy of the hybrid metal oxide cycle of FIG. 1.

DETAILED DESCRIPTION

Hybrid thermochemical water splitting cycles are proposed in which thermally reduced metal oxides particles are used to displace some but not all of the electrical requirements in a water splitting electrolytic cell. In these hybrid cycles, the thermal reduction temperature is significantly reduced compared to two-step metal-oxide thermochemical cycles in which only thermal energy is required to produce hydrogen from water. Also, unlike the conventional higher temperature cycles where the reduction step must be carried out under reduced oxygen pressure, the reduction step in the proposed hybrid cycles can be (but are not required to be) carried out in air, allowing for thermal input by a solar power tower with a windowless, cavity receiver. These proposed hybrid cycles could also potentially enable the use of heat from a nuclear reactor. Regardless of the energy input source, solar or nuclear, in the hybrid scheme the products from thermal reduction are utilized as a chemically active anode material in a water splitting electrolyzer. Because the anode is re-oxidized during electrolysis, the electrical input required to split water is reduced substantially below the electric input required to drive a conventional water splitting electrolyzer. For example, the ideal decomposition voltage can drop from the 1.23 volts needed in a conventional cell to values as low as 0.23 volts. This approach appears well suited to an electrolyzer where the anode is a packed or moving (possibly fluidized) bed of particles. The bed could either be stand-alone, or could be a mixture of a conductor, e.g. Ni metal, and the solar reduced oxide. This cell design concept could be integrated with a reactive-particle solid particle receiver. Appropriate sizing of the receiver relative to the electrolyzer would allow for round-the-clock continuous operation of the electrolyzer.

Thermochemical cycles are an attractive alternative to electrolysis as they have the potential for higher energy efficiency due to the fact that they avoid the need to first convert thermal energy into electrical energy. There are many proposed metal oxide thermochemical cycles for water splitting. For example, the Iron Oxide cycle is one that has been interesting to the research community because the reduced iron oxide is capable of reacting with water to produce hydrogen. However, in this cycle very high temperatures are needed to thermally reduce magnetite, Fe₃O₄, to the reduced oxide, wustite, FeO. Complicating matters is the fact that the recovery of FeO is dependent on the reduction step being conducted under reduced oxygen partial pressure, e.g. in a vacuum or in the presence of an inert sweep gas. Also, the oxides melt and are somewhat volatile at the required temperatures. The thermodynamic high temperature requirements and thermodynamic and kinetic requirements forcing the reaction to take place under an inert atmosphere as well as numerous materials challenges posed for these types of cycles compromise significantly the potential of engineering these cycles into an efficient and industrially economically realizable process. We are, therefore, interested in processes where the thermal reduction step can be done at temperatures below 1500° C. and even in air.

As an example, oxygen can be driven off from cobalt and manganese oxides (i.e. Co₃O₄ MnO₂, and Mn₂O₃) at significantly lower temperatures than needed to thermally reduce magnetite. In addition, oxygen can also be produced from hematite, Fe₂O₃, at much lower temperatures. 3Fe₂O₃→2Fe₃O₄+½O₂  (1)

The factor previously eliminating the use of these attractive thermal reduction chemistries has been the other half of the two-step cycle. The Gibbs free energy, ΔG, of the oxidation Fe₃O₄ and the thermally reduced states of cobalt and manganese oxides with water are positive at any temperature above and including room temperature. That is, they are thermodynamically stable in the presence of water and steam, and will not spontaneously oxidize to yield hydrogen. (Note: Because the reaction with water is not favorable, steam is essentially inert in the system and could be employed gainfully as a sweep to promote the reduction reaction if desired).

The factor previously eliminating the use of these attractive thermal reduction chemistries has been the other half of the two-step cycle. The Gibbs free energy, ΔG, of the oxidation Fe₃O₄ and the thermally reduced states of cobalt and manganese oxides with water are positive at any temperature above and including room temperature. That is, they are thermodynamically stable in the presence of water and steam, and will not spontaneously oxidize to yield hydrogen. (Note: Because the reaction with water is not favorable, steam is essentially inert in the system and could be employed gainfully as a sweep to promote the reduction reaction if desired). 2Fe₃O₄+H₂O(g)→3Fe₂O₃+H₂(g) ΔG>0  (2)

Employing a third reaction with sodium hydroxide or potassium hydroxide has been proposed to make the oxidation thermodynamics favorable for metal oxide cycles in which the oxidation reaction is not favorable However, the addition of the third reaction step and the addition of hydroxides significantly complicate the cycles. A key insight is that these oxidation reactions can be made favorable and the complications of a third step eliminated with the addition of only a small applied voltage at ambient temperature, one significantly less than that required for conventional electrolysis. 2Fe₃O₄+H₂O(g)+Power (IV)→3Fe₂O₃+H₂(g) ΔG<0  (3)

Comparison to Alternate Approaches:

The proposed hybrid cycle 10, shown schematically in FIG. 1, is similar to conventional two-step thermochemical cycles with the exception that the oxidation step is electrochemically assisted. In the hybrid thermochemical cycle 10, a metal oxide 12 is thermally reduced (driving off oxygen 16) with concentrated solar energy 18. The oxygen deficient metal oxide 14 is subsequently reoxidized in an electrochemical cell 20 to reduce water to hydrogen or carbon dioxide to carbon monoxide. Heat 20 extracted from the reduced metal oxide 14 can be used for power generation 22. The chemical potential for the water or carbon dioxide reducing reactions is provided by the reduced metal oxide and electrical energy. The electrical energy is required is significantly lower than needed for water or carbon dioxide electrolysis alone. The payoff for this hybrid approach is that the extreme challenges posed by the ultra-high temperature reduction (e.g. materials degradation, volatilization, limited heat source options, thermal energy management, closed systems with inert gas sweeps, etc.) are exchanged for a simpler electrochemical step. Because the hybrid cycle 10 is significantly more straight forward, it should be much easier to implement and thus in practice should be more efficient than the proposed processes that split water with an exothermic reaction like that corresponding the iron oxide cycle.

Note that in the hybrid approach, the reduction and oxidation steps of two step metal oxide cycles are separated and can be performed independently of each other. An advantage of this is that while the solar driven thermochemical step can be carried out when the sun is available, the electrochemically driven oxidation step can occur when convenient. Therefore, by over-sizing the thermally driven reduction process relative to the electrochemical oxidation process, it is possible to achieve round-the-clock operation. This has the benefit of maximizing the utilization of the electrochemical equipment and minimizing issues associated with starting and stopping the electrochemical reactor.

It may be noted that this metal-oxide hybrid approach is analogous to the Hybrid Sulfur cycle where the hydrogen production step is electrochemical vs. the 3-step Sulfur-Iodine thermochemical cycle. However, the metal oxide approach utilizes no corrosive or hazardous chemicals and utilizes only gas-solid and gas-liquid reactions, making for convenient separations of valuable products from the working materials. It is also worth pointing out that the hybrid process is an alternative to solar thermal electrolysis processes that have been explored over the past thirty years. They were motivated by the fact that the higher the operating temperature of an electrolytic cell the more one could substitute sunlight for valuable electric work. Thus a number of studies show running modestly high solar processes where sunlight and electric energy is simultaneously supplied to the solar reactor. Our hybrid metal oxide cycle 10 is thermodynamically equivalent to this approach, but by separating the electrolytic step from the thermal reduction step, one greatly reduces the complexity of the solar reactor and allows for a quasi-24-hour continuous solar process. The thermodynamics of metal oxide cycles allow for a much higher percentage of thermal vs. electrical contribution to water splitting at lower temperatures, compared to direct high-temperature water electrolysis.

Materials and Thermodynamics:

A non-exclusive list of metal oxides we believe are of interest for this hybrid approach includes Fe₂O₃, MnO₂, Mn₂O₃, and Co₃O₄ where the products from the solar reduction step are Fe₃O₄, MnO, and CoO. By selecting the metal oxides, or perhaps mixed metal oxides, it may be possible to tailor the thermodynamics to a particular temperature range, perhaps enabling application to nuclear power sources or solar power towers. Thus mixed metal oxides, e.g. ferrites of cobalt, nickel, manganese, etc. and similar materials are also of interest as are other families of materials metals with numerous possible valence states such as vanadium, molybdenum, niobium, chrome, tungsten, and cerium-oxides.

Tables 1 and 2 show the thermodynamics of water splitting with a hybrid iron oxide (hematite) cycle. Table 1a showing the reduction of magnetite is provided as a baseline comparison. Clearly, the thermal reduction of hematite is far easier to accomplish. Table 2 shows that only about 10.6 kcal would be needed in a hematite/magnetite hybrid cell where the anode is chemically active whereas about 56.7 kcal of electrical energy is needed to electrochemically split water at room temperature with the traditional inert anode used in electrolyzers; the minimum voltage is reduced to about 0.23 Volts from 1.23 Volts. Tables 3 and 4 show similar calculations with cobalt oxide and Tables 5 and 6 show calculations for one particular manganese oxide couple. For cobalt, the thermal reduction temperature is significantly reduced while the cell voltage is 0.38 Volts, which is still significantly less than needed to electrolyze water directly. For the manganese oxide couple the cell voltage is also about 0.38 volts.

TABLE 1 Thermodynamics of hematite reduction 3Fe₂O₃ = 2Fe₃O₄ + ½O₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 55.509 31.723 46.844 100.000 55.676 32.213 43.656 200.000 55.864 32.666 40.408 300.000 55.976 32.879 37.131 400.000 56.365 33.495 33.818 500.000 57.543 35.109 30.398 600.000 59.194 37.144 26.761 700.000 57.776 35.614 23.118 800.000 57.708 35.545 19.562 900.000 57.565 35.420 16.012 1000.000 57.220 35.139 12.483 1100.000 56.769 34.798 8.986 1200.000 56.286 34.459 5.524 1300.000 55.833 34.161 2.093 1400.000 55.459 33.930 −1.311

TABLE 1a Thermodynamics of magnetite reduction Fe₃O₄ = 3FeO + ½O₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 75.541 30.449 67.224 200.000 75.483 30.508 61.048 400.000 74.380 28.626 55.110 600.000 71.304 24.670 49.763 800.000 70.484 23.800 44.943 1000.000 70.619 23.908 40.181 1200.000 71.130 24.279 35.363 1400.000 88.982 35.116 30.228 1600.000 56.815 17.941 23.208 1800.000 57.297 18.186 19.595 2000.000 57.789 18.412 15.935

TABLE 2 Thermodynamics of water dissociation with magnetite 2Fe₃O₄ + H₂O = 3Fe₂O₃ + H₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 14.431 13.226 10.818 100.000 12.068 5.108 10.161 200.000 11.064 2.722 9.775 300.000 9.895 0.496 9.611 400.000 7.844 −2.786 9.719 500.000 4.961 −6.762 10.189 600.000 1.621 −10.851 11.096 700.000 1.367 −11.134 12.202 800.000 −0.223 −12.687 13.393 900.000 −1.723 −14.026 14.732 1000.000 −3.008 −15.078 16.189

TABLE 3 Thermodynamics of cobalt oxide reduction Co₃O₄ = 3CoO + ½O₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 46.532 33.919 37.267 100.000 47.737 37.726 33.659 200.000 48.516 39.590 29.784 300.000 49.020 40.564 25.770 400.000 49.299 41.017 21.688 500.000 49.365 41.112 17.579 600.000 49.214 40.932 13.475 700.000 48.837 40.525 9.400 800.000 48.218 39.922 5.376 900.000 47.343 39.143 1.422 1000.000 46.193 38.204 −2.447 1100.000 44.750 37.115 −6.214 1200.000 42.997 35.884 −9.865 1300.000 40.914 34.517 −13.387 1400.000 38.483 33.020 −16.765

TABLE 4 Thermodynamics of water dissociation with 3CoO + H₂O(g) = Co₃O₄ + H₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 11.208 −23.507 17.629 100.000 10.238 −26.580 20.156 200.000 9.684 −27.908 22.889 300.000 9.396 −28.469 25.712 400.000 9.323 −28.590 28.568 500.000 9.453 −28.413 31.421 600.000 9.786 −28.010 34.243 700.000 10.332 −27.420 37.016 800.000 11.103 −26.668 39.722 900.000 12.114 −25.769 42.345 1000.000 13.382 −24.734 44.871

TABLE 5 Thermodynamics of manganese oxide reduction 2Mn₂O₃ = 4MnO + O₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 44.529 26.551 37.277 100.000 44.597 26.773 34.607 200.000 44.571 26.713 31.931 300.000 44.493 26.566 29.267 400.000 44.379 26.382 26.619 500.000 44.231 26.178 23.991 600.000 44.049 25.957 21.384 700.000 43.829 25.720 18.800 800.000 43.570 25.466 16.241 900.000 43.266 25.195 13.708 1000.000 42.913 24.907 11.203 1100.000 42.509 24.602 8.727 1200.000 42.048 24.278 6.283 1300.000 41.527 23.936 3.872 1400.000 40.942 23.576 1.496 1500.000 40.289 23.197 −0.843

TABLE 6 Thermodynamics of water dissociation with 2MnO + H₂O(g) = Mn₂O₃ + H₂(g) T, ° C. deltaH, kcal deltaS, cal/K deltaG, kcal 0.000 13.210 −16.139 17.618 100.000 13.378 −15.626 19.208 200.000 13.629 −15.031 20.741 300.000 13.922 −14.470 22.216 400.000 14.243 −13.955 23.637 500.000 14.587 −13.479 25.008 600.000 14.952 −13.036 26.334 700.000 15.339 −12.615 27.616 800.000 15.752 −12.212 28.857 900.000 16.191 −11.821 30.059 1000.000 16.661 −11.437 31.222

Example Implementation Strategy:

An example implementation strategy 40 is shown in FIG. 2. The oxygen producing step in the hybrid metal oxide cycle is thermally driven. A preferred method could be in a reactive particle receiver 42. In the reactive particle solar receiver 42, the oxidized particles would be directly heated and thermally reduced in an open cavity 44, potentially in air. The reactive particle solar receiver 42 is similar to the solid particle receiver except that the particles undergo thermal reduction chemical reactions in the receiver. The particles could be recirculated within the receiver to increase residence and heat transfer times. The use of inert gas such a nitrogen (it would not require high purity) inside the reactive particle receiver/reactor cavity 46 could further drive the reaction and/or lower the temperatures required. Countercurrent flow of the metal oxide particles and inert gas in the down comer 48 of the reactive particle receiver 42 would be advantageous for driving the thermal reduction reaction with some of the sensible heat in the particles. The hot (reduced) metal oxides could be used to preheat the metal oxide feed. As shown in FIG. 2, an alternative would be to use the sensible thermal energy to drive electricity producing Rankine or other thermodynamic cycle before being fed to the electrochemical cell. Low-grade steam exiting the Rankine cycle could also be employed as an inert sweep in the reactive solid particle receiver.

We envision that the reduced particles would be fed into the electrolyzer as a slurry in water. The slurry may also contain an electrolyte such as potassium hydroxide. This electrochemical step may be facilitated by packed bed or fluidized bed electrodes, an approach that has received a significant amount of research. In this concept the reduced metal oxide, mixed or doped with a kinetically oxygen-inert electrically conductive material, such as Ni, would be the cell's anode. The metal oxide is the active anode and the Ni is facilitating the needed electron transfer for the anodic reaction to take place, but is not chemically participating in the reaction. The required electrochemical potential needed to split water is reduced in comparison to the required potential of a traditional electrolysis of water by the chemical potential from the metal oxide. The active anode, however, is consumed as it is oxidized during the electrolysis process and would be circulated through the electrolytic cell. After leaving the electrolytic cell the reoxidized metal oxide particles would be rinsed to remove the electrolyte and dried before returning to the reactive particle receiver.

Other Embodiments

Other analogous redox reactions are candidates for a similar approach. For example, the splitting of CO₂ to CO and O₂ should be amenable to same approach and materials outlined here.

The hybrid electrochemical approach could also be used to enhance the oxidation kinetics of systems wherein the reactions are thermodynamically favorable, but are reaction rate limited.

It is contemplated that the parts and features of any one of the specific embodiments described can be interchanged with the parts and features of any other of the embodiments without departing from the spirit and scope of the present disclosure. The foregoing description discloses and describes merely exemplary embodiments of the present disclosure and is not intended to be exhaustive or to limit the disclosure to the precise form disclosed. As will be understood by those skilled in the art, the disclosure may be embodied in other specific forms, or modified or varied in light of the above teachings, without departing from the spirit, novelty or essential characteristics of the present disclosure. Accordingly, the disclosed embodiments are intended to be illustrative, but not limiting, of the scope of the invention. The exclusive right to all modifications within the scope of this disclosure is reserved. 

What is claimed is:
 1. A hybrid thermochemical splitting cycle implementation comprising: a reactive particle receiver including an open cavity; a down comer; a hot particle storage container; a heat exchanger; and an electrolyzer; wherein oxidized particles are directly heated and thermally reduced in the open cavity.
 2. The hybrid thermochemical splitting cycle implementation of claim 1, wherein the oxidized particles are recirculated within the reactive particle receiver to increase residence and heat transfer times.
 3. The hybrid thermochemical splitting cycle implementation of claim 1, wherein particles within the reactive particle receiver are recirculated within the reactive particle receiver to increase residence time.
 4. The hybrid thermochemical splitting cycle implementation of claim 1, wherein the open cavity receives concentrated solar flux.
 5. The hybrid thermochemical splitting cycle implementation of claim 1, further comprising: an electric power cycle in thermal connectivity with the heat exchanger that receives heat removed by the heat exchanger.
 6. The hybrid thermochemical splitting cycle implementation of claim 1, wherein the electrolyzer is configured to reoxidize an oxygen-deficient metal oxide by reducing water to produce hydrogen.
 7. The hybrid thermochemical splitting cycle implementation of claim 6, wherein the electrolyzer is further configured to receive electricity for reducing water into hydrogen.
 8. The hybrid thermochemical splitting cycle implementation of claim 1, wherein the electrolyzer is configured to reoxidize an oxygen-deficient meal oxide by reducing carbon dioxide to produce carbon monoxide.
 9. The hybrid thermochemical splitting cycle implementation of claim 8, wherein the electrolyzer is further configured to receive electricity for reducing carbon dioxide to produce hydrogen. 